Document Detail


Critical role of allyl groups and disulfide chain in induction of Pi class glutathione transferase in mouse tissues in vivo by diallyl disulfide, a naturally occurring chemopreventive agent in garlic.
MedLine Citation:
PMID:  12376475     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We have shown previously that the chemoprotective activity of diallyl disulfide (DADS), a naturally occurring anticancer agent in garlic, against benzo[a]pyrene (BP)-induced forestomach carcinogenesis in mice correlates strongly with its inductive effects on the expression of Pi class glutathione (GSH) transferase mGSTP1-1. The present structure-activity relationship studies were designed to define the role of allyl groups and the disulfide chain in mGSTP1-inducing activity of DADS. Hepatic mGSTP1 mRNA levels rose rapidly upon treatment of mice with DADS, reached a maximum between 12 and 24 h (< or =5.7-fold induction) and fell to control levels by 48 h after DADS treatment. Induction of mGSTP1 mRNA in the forestomach was maximal between 6 and 12 h after DADS treatment (< or =4.7-fold induction). The mGSTP1 mRNA expression was either unaltered (liver) or moderately increased (forestomach) upon treatment of mice with dipropyl disulfide (DPDS), which is a naturally occurring saturated analog of DADS. These results indicated that the allyl groups are critical for the mGSTP1-inducing activity of DADS. A statistically significant increase in the expression of mGSTP1 mRNA was also observed in the liver and forestomach of mice treated with diallyl monosulfide (DAMS), albeit to a much lesser extent compared with DADS. These results indicated that the oligosulfide chain length in garlic organosulfides (OSCs) is equally important for their mGSTP1-inducing activity. The role of the disulfide chain in DADS-mediated induction of mGSTP1 was further investigated by testing a pair of alkadienes (1,7-octadiene and 1,8-nonadiene) having structural similarity to DADS. Both DADS and the alkadienes carry allyl groups at both ends of a linear molecule and the distance between the allylic carbon atoms is similar in both compounds, but the central disulfide chain of DADS is replaced with an alkyl chain in the alkadienes. The alkadienes were either ineffective or moderately active in increasing mGSTP1 expression. In conclusion, the results of the present study clearly indicate that the presence of terminal allyl groups as well as the central disulfide chain is required for maximum induction of mGSTP1 in vivo by garlic-derived OSCs.
Authors:
Chhanda Bose; Jianxia Guo; Ludwika Zimniak; Sanjay K Srivastava; Sharda P Singh; Piotr Zimniak; Shivendra V Singh
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Carcinogenesis     Volume:  23     ISSN:  0143-3334     ISO Abbreviation:  Carcinogenesis     Publication Date:  2002 Oct 
Date Detail:
Created Date:  2002-10-11     Completed Date:  2002-11-22     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8008055     Medline TA:  Carcinogenesis     Country:  England    
Other Details:
Languages:  eng     Pagination:  1661-5     Citation Subset:  IM    
Affiliation:
Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
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MeSH Terms
Descriptor/Qualifier:
Allyl Compounds / chemistry,  pharmacology*
Animals
Anticarcinogenic Agents / pharmacology*
Carcinogens
Disulfides / chemistry,  pharmacology*
Female
Garlic*
Glutathione S-Transferase pi
Glutathione Transferase / genetics*
Isoenzymes / genetics*
Kinetics
Liver / drug effects,  enzymology
Mice
Mice, Inbred A
Phytotherapy*
RNA, Messenger / genetics
Structure-Activity Relationship
Transcription, Genetic / drug effects
Grant Support
ID/Acronym/Agency:
CA55589/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
0/Allyl Compounds; 0/Anticarcinogenic Agents; 0/Carcinogens; 0/Disulfides; 0/Isoenzymes; 0/RNA, Messenger; 2179-57-9/diallyl disulfide; EC 2.5.1.18/Glutathione S-Transferase pi; EC 2.5.1.18/Glutathione Transferase; EC 2.5.1.18/Gstp1 protein, mouse

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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